Berardinelli-Seip Congenital Lipodystrophy 2 (Seipin) (BSCL2) (C-Term) Peptid
BSCL2
Reaktivität: Human
Wirt: Synthetic
BP, WB
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- Target Alle BSCL2 Produkte
- BSCL2 (Berardinelli-Seip Congenital Lipodystrophy 2 (Seipin) (BSCL2))
- Protein Region
- C-Term
- Spezies
- Human
-
Quelle
- Synthetic
- Applikation
- Blocking Peptide (BP), Western Blotting (WB)
- Sequenz
- QEESTPQSDV TEDGESPEDP SGTEGQLSEE EKPDQQPLSG EEELEPEAS
- Produktmerkmale
- This is a synthetic peptide designed for use in combination with anti-BSCL2 Antibody(ARP50102_P050),. It may block above mentioned antibody from binding to its target protein in western blot and/or immunohistochecmistry under proper experimental settings. There is no guarantee for its use in other applications.
- Aufreinigung
- Purified
-
-
- Applikationshinweise
- Each Investigator should determine their own optimal working dilution for specific applications.
- Beschränkungen
- Nur für Forschungszwecke einsetzbar
-
- Format
- Lyophilized
- Rekonstitution
- Add 100 μL of sterile PBS. Final peptide concentration is 1 mg/mL in PBS.
- Konzentration
- 1 mg/mL
- Buffer
- Final peptide concentration is 1 mg/mL in PBS.
- Handhabung
- Avoid repeated freeze-thaw cycles.
- Lagerung
- -20 °C
- Informationen zur Lagerung
- For longer periods of storage, store at -20°C. Avoid repeat freeze-thaw cycles.
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- Target
- BSCL2 (Berardinelli-Seip Congenital Lipodystrophy 2 (Seipin) (BSCL2))
- Synonyme
- GNG3LG Peptide, HMN5 Peptide, SPG17 Peptide, 2900097C17Rik Peptide, AI046355 Peptide, Gng3lg Peptide, BSCL2, seipin lipid droplet biogenesis associated Peptide, Berardinelli-Seip congenital lipodystrophy 2 (seipin) Peptide, BSCL2 Peptide, Bscl2 Peptide
- Hintergrund
-
This gene encodes protein seipin, which is located in the endoplasmic reticulum and may be important for lipid droplet morphology. Mutations in this gene have been associated with congenital generalized lipodystrophy type 2 or Berardinelli-Seip syndrome, a rare autosomal recessive disease characterized by a near absence of adipose tissue and severe insulin resistance. Alternatively spliced transcript variants encoding different isoforms have been found for this gene.
Alias Symbols: GNG3LG, HMN5, MGC4694, SPG17
Protein Interaction Partner: C5orf62,TMEM19,USE1,C5orf62,CANX,TMEM19,UBC,USE1
Protein Size: 462 - Molekulargewicht
- 51 kDa
- Gen-ID
- 26580
- NCBI Accession
- NM_001122955, NP_001116427
- UniProt
- Q96G97
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